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Osborn Group, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K002156
APPRAISE URINE MICROALBUMIN COLLECTION KIT
December 19, 2000
K993787
APPRAISE-CARDIO SAMPLE COLLECTION KIT
April 14, 2000
K990899
HEMOCHEK-A1C SAMPLE COLLECTION KIT
December 21, 1999
K991800
HEMOCHEK URINE COLLECTION KIT
September 24, 1999